SNAR-B1

Summary

SNAR-B1 (small NF90 (ILF3) associated RNA B1, HGNC:34317) is a gene on chromosome 19q13.33.

Predicted to be located in cytoplasm and nucleus.

Source: NCBI Gene 100170224 — RefSeq curated summary.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:34317
Approved symbol	SNAR-B1
Name	small NF90 (ILF3) associated RNA B1
Location	19q13.33
Locus type	RNA, misc
Status	Approved
Entrez	100170224
RNAcentral	URS000002A4F1 — ncRNA, 120 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 0

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

None — 0 exons

Expression profiles

Top tissues by expression

0 total, by Bgee expression score (0-100, higher = more expressed):

Regulation

Is transcription factor: no

Cross-species orthologs

0 orthologs

Protein

Protein identifiers

Canonical reviewed UniProt: None (reviewed: )

All UniProt accessions (0):

RefSeq proteins (0): (*=MANE)

Domains & families (InterPro)

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 0 (showing top):

GO Biological Process (0):

GO Molecular Function (0):

GO Cellular Component (0):

Protein interactions and networks

STRING

0 interactions, top by confidence (×1000):

IntAct

0 interactions, top by confidence:

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

0 variants total. Per-class counts are floors (≥ shown; pagination cap):

Classification	Count (floor)
Pathogenic	0
Likely pathogenic	0
Uncertain significance	0
Likely benign	0
Benign	0

Top pathogenic / likely-pathogenic (0)

SpliceAI

0 predictions. Top by Δscore:

AlphaMissense

0 scored. Top likely-pathogenic:

dbSNP variants (sampled 300 via entrez): RS1011986778 (19:50134000 A>C,G), RS1023085469 (19:50134275 C>T), RS1035542983 (19:50135243 G>A), RS1156319675 (19:50135188 C>CGGGG), RS1158318730 (19:50134482 G>A,T), RS1158495492 (19:50133849 G>A), RS1159533409 (19:50134117 C>G), RS1159600460 (19:50133967 G>A), RS1159682653 (19:50134948 T>G), RS1159899639 (19:50135642 GT>G,GTT), RS1160203292 (19:50134362 C>G,T), RS1161798794 (19:50133876 G>A,C), RS1161930623 (19:50134541 A>C,G), RS1164025182 (19:50133718 C>A), RS1164057534 (19:50134191 G>A,C)

Disease associations

OMIM: gene `` | disease phenotypes:

GenCC curated gene-disease

Mondo (0):

Orphanet (0):

HPO phenotypes

0 total (0 of 0 shown, HPO-id order):

GWAS associations

0 associations (top):

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

PharmGKB: 1 entry (VIP=true, CPIC=false)

CTD chemical–gene interactions

1 total (human), top 1 by PubMed support.

Chemical	Actions (top 5)	PubMed papers
Benzo(a)pyrene	increases methylation	1

Clinical trials (associated diseases)

0 trials via MONDO — disease-level, not drug-specific.